JP2008528451A5 - - Google Patents
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- JP2008528451A5 JP2008528451A5 JP2007551527A JP2007551527A JP2008528451A5 JP 2008528451 A5 JP2008528451 A5 JP 2008528451A5 JP 2007551527 A JP2007551527 A JP 2007551527A JP 2007551527 A JP2007551527 A JP 2007551527A JP 2008528451 A5 JP2008528451 A5 JP 2008528451A5
- Authority
- JP
- Japan
- Prior art keywords
- ester
- group
- ethyl
- acetyl
- hydroxy
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 150000001875 compounds Chemical class 0.000 claims description 7
- -1 R 9 Chemical compound 0.000 claims description 6
- FGOJCPKOOGIRPA-UHFFFAOYSA-N 1-o-tert-butyl 4-o-ethyl 5-oxoazepane-1,4-dicarboxylate Chemical compound CCOC(=O)C1CCN(C(=O)OC(C)(C)C)CCC1=O FGOJCPKOOGIRPA-UHFFFAOYSA-N 0.000 claims description 5
- 235000010357 aspartame Nutrition 0.000 claims description 5
- VPNLWAHMLQRTKB-UHFFFAOYSA-N 4-o-ethyl 1-o-(2-methoxyethyl) 2-acetylbut-2-enedioate Chemical compound CCOC(=O)C=C(C(C)=O)C(=O)OCCOC VPNLWAHMLQRTKB-UHFFFAOYSA-N 0.000 claims description 3
- CMKNNYLWGWYZGD-UHFFFAOYSA-N dibenzyl 2-octylidenepropanedioate Chemical compound C=1C=CC=CC=1COC(=O)C(=CCCCCCCC)C(=O)OCC1=CC=CC=C1 CMKNNYLWGWYZGD-UHFFFAOYSA-N 0.000 claims description 3
- UJLZHPXERCRUAA-UHFFFAOYSA-N diethyl 2-butanoylbut-2-enedioate Chemical compound CCCC(=O)C(C(=O)OCC)=CC(=O)OCC UJLZHPXERCRUAA-UHFFFAOYSA-N 0.000 claims description 3
- TZBUSAJVQQGGFP-UHFFFAOYSA-N ethyl 2-acetyl-5,9-dimethyldeca-2,8-dienoate Chemical compound CCOC(=O)C(C(C)=O)=CCC(C)CCC=C(C)C TZBUSAJVQQGGFP-UHFFFAOYSA-N 0.000 claims description 3
- BKULVIZFOHJLLV-UHFFFAOYSA-N ethyl 2-benzoyldec-2-enoate Chemical compound CCCCCCCC=C(C(=O)OCC)C(=O)C1=CC=CC=C1 BKULVIZFOHJLLV-UHFFFAOYSA-N 0.000 claims description 3
- FFPHIZSVBKYWOQ-UHFFFAOYSA-N ethyl 3-(4-methylcyclohexanecarbonyl)-4-oxopent-2-enoate Chemical compound CCOC(=O)C=C(C(C)=O)C(=O)C1CCC(C)CC1 FFPHIZSVBKYWOQ-UHFFFAOYSA-N 0.000 claims description 3
- PIMSKFUWNYECEL-UHFFFAOYSA-N ethyl 3-(cyclohexanecarbonyl)-4-oxopent-2-enoate Chemical compound CCOC(=O)C=C(C(C)=O)C(=O)C1CCCCC1 PIMSKFUWNYECEL-UHFFFAOYSA-N 0.000 claims description 3
- RBSPMIQCMGHSNU-UHFFFAOYSA-N ethyl 3-carbamoyl-4-oxopent-2-enoate Chemical compound CCOC(=O)C=C(C(C)=O)C(N)=O RBSPMIQCMGHSNU-UHFFFAOYSA-N 0.000 claims description 3
- IDYUUEKAPPIYBR-UHFFFAOYSA-N ethyl 4-oxo-3-(trimethylsilylmethylcarbamoyl)pent-2-enoate Chemical compound CCOC(=O)C=C(C(C)=O)C(=O)NC[Si](C)(C)C IDYUUEKAPPIYBR-UHFFFAOYSA-N 0.000 claims description 3
- VKTPASXYRPGXFL-UHFFFAOYSA-N methyl 2-carbamoyldec-2-enoate Chemical compound CCCCCCCC=C(C(N)=O)C(=O)OC VKTPASXYRPGXFL-UHFFFAOYSA-N 0.000 claims description 3
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 3
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 3
- WZQPCWQUUMNLBF-UHFFFAOYSA-N 2-(2-methoxyethoxy)ethyl 2-acetyldec-2-enoate Chemical compound CCCCCCCC=C(C(C)=O)C(=O)OCCOCCOC WZQPCWQUUMNLBF-UHFFFAOYSA-N 0.000 claims description 2
- IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 claims description 2
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 19
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 19
- 229910052757 nitrogen Inorganic materials 0.000 claims 18
- 229910052794 bromium Inorganic materials 0.000 claims 17
- 239000000460 chlorine Substances 0.000 claims 17
- 229910052801 chlorine Inorganic materials 0.000 claims 17
- 125000005842 heteroatom Chemical group 0.000 claims 17
- 229910052710 silicon Inorganic materials 0.000 claims 17
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 16
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 16
- 229910052760 oxygen Inorganic materials 0.000 claims 16
- 125000004185 ester group Chemical group 0.000 claims 15
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 12
- 125000001033 ether group Chemical group 0.000 claims 10
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 9
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 9
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims 9
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 9
- 239000010703 silicon Substances 0.000 claims 9
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 8
- 239000001301 oxygen Substances 0.000 claims 8
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims 4
- 125000003118 aryl group Chemical group 0.000 claims 4
- 229910052799 carbon Inorganic materials 0.000 claims 4
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 claims 4
- WRTHUMPHVMGUOC-UHFFFAOYSA-N 1-o-ethyl 4-o-(2-methoxyethyl) 3-acetyl-2-hydroxybutanedioate Chemical compound CCOC(=O)C(O)C(C(C)=O)C(=O)OCCOC WRTHUMPHVMGUOC-UHFFFAOYSA-N 0.000 claims 3
- 125000000217 alkyl group Chemical group 0.000 claims 3
- 125000001424 substituent group Chemical group 0.000 claims 3
- PSHSMSYSLFPJEN-NTMALXAHSA-N 1-o-[2-(dimethylamino)ethyl] 4-o-ethyl (z)-2-acetylbut-2-enedioate Chemical compound CCOC(=O)\C=C(\C(C)=O)C(=O)OCCN(C)C PSHSMSYSLFPJEN-NTMALXAHSA-N 0.000 claims 2
- QNYTXFASIYXTPM-UHFFFAOYSA-N 1-o-benzyl 4-o-ethyl 2-acetylbut-2-enedioate Chemical compound CCOC(=O)C=C(C(C)=O)C(=O)OCC1=CC=CC=C1 QNYTXFASIYXTPM-UHFFFAOYSA-N 0.000 claims 2
- 125000006374 C2-C10 alkenyl group Chemical group 0.000 claims 2
- 125000005865 C2-C10alkynyl group Chemical group 0.000 claims 2
- 125000001313 C5-C10 heteroaryl group Chemical group 0.000 claims 2
- 125000002877 alkyl aryl group Chemical group 0.000 claims 2
- 125000005119 alkyl cycloalkyl group Chemical group 0.000 claims 2
- 150000001721 carbon Chemical group 0.000 claims 2
- 239000011203 carbon fibre reinforced carbon Substances 0.000 claims 2
- HOHCZDBRLMYZMU-UHFFFAOYSA-N diethyl 2-acetyl-3-hydroxybutanedioate Chemical compound CCOC(=O)C(O)C(C(C)=O)C(=O)OCC HOHCZDBRLMYZMU-UHFFFAOYSA-N 0.000 claims 2
- CZBMCQVEYULJOE-UHFFFAOYSA-N diethyl 2-benzoyl-3-ethoxybutanedioate Chemical compound CCOC(=O)C(OCC)C(C(=O)OCC)C(=O)C1=CC=CC=C1 CZBMCQVEYULJOE-UHFFFAOYSA-N 0.000 claims 2
- YMUBTSFQIVTHJU-UHFFFAOYSA-N diethyl 2-benzoyl-3-hydroxybutanedioate Chemical compound CCOC(=O)C(O)C(C(=O)OCC)C(=O)C1=CC=CC=C1 YMUBTSFQIVTHJU-UHFFFAOYSA-N 0.000 claims 2
- SLLDNQSYNKTVFD-UHFFFAOYSA-N diethyl 2-butanoyl-3-ethoxybutanedioate Chemical compound CCCC(=O)C(C(=O)OCC)C(OCC)C(=O)OCC SLLDNQSYNKTVFD-UHFFFAOYSA-N 0.000 claims 2
- YQUQINJSZJWENV-UHFFFAOYSA-N ethyl 3-acetyl-2-hydroxy-4-oxopentanoate Chemical compound CCOC(=O)C(O)C(C(C)=O)C(C)=O YQUQINJSZJWENV-UHFFFAOYSA-N 0.000 claims 2
- RGNHIESYGXQDQU-UHFFFAOYSA-N ethyl 3-benzoyl-2-ethoxy-4-oxopentanoate Chemical compound CCOC(=O)C(OCC)C(C(C)=O)C(=O)C1=CC=CC=C1 RGNHIESYGXQDQU-UHFFFAOYSA-N 0.000 claims 2
- 239000000758 substrate Substances 0.000 claims 2
- OARZICFFWXUUQS-UHFFFAOYSA-N 1-(4-tert-butylphenyl)-3-(4-methoxyphenyl)-2-octylidenepropane-1,3-dione Chemical compound C=1C=C(C(C)(C)C)C=CC=1C(=O)C(=CCCCCCCC)C(=O)C1=CC=C(OC)C=C1 OARZICFFWXUUQS-UHFFFAOYSA-N 0.000 claims 1
- GFDJYEMYBMLSJH-UHFFFAOYSA-N 2-[(2-hydroxyphenyl)methylidene]-1-phenylbutane-1,3-dione Chemical compound C=1C=CC=CC=1C(=O)C(C(=O)C)=CC1=CC=CC=C1O GFDJYEMYBMLSJH-UHFFFAOYSA-N 0.000 claims 1
- KSZCHEAEUSLGEG-UHFFFAOYSA-N 2-acetyldec-2-enoic acid Chemical compound CCCCCCCC=C(C(C)=O)C(O)=O KSZCHEAEUSLGEG-UHFFFAOYSA-N 0.000 claims 1
- ITLGHAXXSHESNE-UHFFFAOYSA-N 2-ethylidene-1-(1h-imidazol-5-yl)butane-1,3-dione Chemical compound CC=C(C(C)=O)C(=O)C1=CN=CN1 ITLGHAXXSHESNE-UHFFFAOYSA-N 0.000 claims 1
- VKPIBFFBMFUIPU-UHFFFAOYSA-N 2-propylidene-1-pyridin-4-ylbutane-1,3-dione Chemical compound CCC=C(C(C)=O)C(=O)C1=CC=NC=C1 VKPIBFFBMFUIPU-UHFFFAOYSA-N 0.000 claims 1
- CHFYBELVXMHVGR-UHFFFAOYSA-N 3-[(2-hydroxy-4-methoxyphenyl)methylidene]pentane-2,4-dione Chemical compound COC1=CC=C(C=C(C(C)=O)C(C)=O)C(O)=C1 CHFYBELVXMHVGR-UHFFFAOYSA-N 0.000 claims 1
- NTFHVYNGNLOVQX-UHFFFAOYSA-N 3-[(2-hydroxy-5-nitrophenyl)methylidene]pentane-2,4-dione Chemical compound CC(=O)C(C(C)=O)=CC1=CC([N+]([O-])=O)=CC=C1O NTFHVYNGNLOVQX-UHFFFAOYSA-N 0.000 claims 1
- DDMYUHBSCSXTAY-UHFFFAOYSA-N 3-[(2-hydroxyphenyl)methylidene]pentane-2,4-dione Chemical compound CC(=O)C(C(C)=O)=CC1=CC=CC=C1O DDMYUHBSCSXTAY-UHFFFAOYSA-N 0.000 claims 1
- MJIRAKVJINGAOF-UHFFFAOYSA-N 3-[(3-ethoxy-4-hydroxyphenyl)methylidene]pentane-2,4-dione Chemical compound CCOC1=CC(C=C(C(C)=O)C(C)=O)=CC=C1O MJIRAKVJINGAOF-UHFFFAOYSA-N 0.000 claims 1
- JLFKCZFGOQIKLA-UHFFFAOYSA-N 3-[(5-acetyl-2-hydroxyphenyl)methylidene]pentane-2,4-dione Chemical compound CC(=O)C(C(C)=O)=CC1=CC(C(C)=O)=CC=C1O JLFKCZFGOQIKLA-UHFFFAOYSA-N 0.000 claims 1
- DOMCVUKCALENDA-UHFFFAOYSA-N 3-octylidenepentane-2,4-dione Chemical compound CCCCCCCC=C(C(C)=O)C(C)=O DOMCVUKCALENDA-UHFFFAOYSA-N 0.000 claims 1
- STQAEANNWDXTAD-UHFFFAOYSA-N 4-acetyl-9-methyldeca-3,8-diene-2,5-dione Chemical compound CC(C)=CCCC(=O)C(C(C)=O)=CC(C)=O STQAEANNWDXTAD-UHFFFAOYSA-N 0.000 claims 1
- SCHBZNAIVCKWDG-UHFFFAOYSA-N 4-o-tert-butyl 1-o-ethyl 3-acetyl-2-hydroxybutanedioate Chemical compound CCOC(=O)C(O)C(C(C)=O)C(=O)OC(C)(C)C SCHBZNAIVCKWDG-UHFFFAOYSA-N 0.000 claims 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 claims 1
- IFOLIMZSBBYWRW-UHFFFAOYSA-N benzyl 3-acetyl-4-oxopent-2-enoate Chemical compound CC(=O)C(C(C)=O)=CC(=O)OCC1=CC=CC=C1 IFOLIMZSBBYWRW-UHFFFAOYSA-N 0.000 claims 1
- 125000004663 dialkyl amino group Chemical group 0.000 claims 1
- UDFKZBBVSIDXIL-UHFFFAOYSA-N diethyl 2-(3,7-dimethylocta-2,6-dienylidene)propanedioate Chemical compound CCOC(=O)C(C(=O)OCC)=CC=C(C)CCC=C(C)C UDFKZBBVSIDXIL-UHFFFAOYSA-N 0.000 claims 1
- JHJQXGCGLVPNQX-UHFFFAOYSA-N diethyl 2-(acetyloxymethylidene)propanedioate Chemical compound CCOC(=O)C(=COC(C)=O)C(=O)OCC JHJQXGCGLVPNQX-UHFFFAOYSA-N 0.000 claims 1
- YXXFRMBHUWKHHO-UHFFFAOYSA-N diethyl 2-(ethoxycarbonyloxymethylidene)propanedioate Chemical compound CCOC(=O)OC=C(C(=O)OCC)C(=O)OCC YXXFRMBHUWKHHO-UHFFFAOYSA-N 0.000 claims 1
- DYLWMPQUPUHXOE-UHFFFAOYSA-N diethyl 2-(pyridin-2-ylmethylidene)propanedioate Chemical compound CCOC(=O)C(C(=O)OCC)=CC1=CC=CC=N1 DYLWMPQUPUHXOE-UHFFFAOYSA-N 0.000 claims 1
- HHWFOKLILKCKTC-UHFFFAOYSA-N diethyl 2-[(2-hydroxyphenyl)methylidene]propanedioate Chemical compound CCOC(=O)C(C(=O)OCC)=CC1=CC=CC=C1O HHWFOKLILKCKTC-UHFFFAOYSA-N 0.000 claims 1
- XUMZMKRVRIJEMR-UHFFFAOYSA-N diethyl 2-acetyl-3-[2-(2-ethoxyethoxy)ethoxy]butanedioate Chemical compound CCOCCOCCOC(C(=O)OCC)C(C(C)=O)C(=O)OCC XUMZMKRVRIJEMR-UHFFFAOYSA-N 0.000 claims 1
- ATOPVVXJWMMBEG-UHFFFAOYSA-N diethyl 2-acetyl-3-methoxybutanedioate Chemical compound CCOC(=O)C(OC)C(C(C)=O)C(=O)OCC ATOPVVXJWMMBEG-UHFFFAOYSA-N 0.000 claims 1
- KZROWENHXNDNOJ-UHFFFAOYSA-N diethyl 2-butanoyl-3-hydroxybutanedioate Chemical compound CCCC(=O)C(C(=O)OCC)C(O)C(=O)OCC KZROWENHXNDNOJ-UHFFFAOYSA-N 0.000 claims 1
- OOCVMBSWVBDRPH-UHFFFAOYSA-N diethyl 2-decylidenepropanedioate Chemical compound CCCCCCCCCC=C(C(=O)OCC)C(=O)OCC OOCVMBSWVBDRPH-UHFFFAOYSA-N 0.000 claims 1
- VFUIBCJBPVYRNW-UHFFFAOYSA-N diethyl 2-octylidenepropanedioate Chemical compound CCCCCCCC=C(C(=O)OCC)C(=O)OCC VFUIBCJBPVYRNW-UHFFFAOYSA-N 0.000 claims 1
- ODHIUCXWGBUWRF-UHFFFAOYSA-N dimethyl 2-octylidenepropanedioate Chemical compound CCCCCCCC=C(C(=O)OC)C(=O)OC ODHIUCXWGBUWRF-UHFFFAOYSA-N 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- GZFRHJPONRZEKP-UHFFFAOYSA-N ethyl 2-[(2-hydroxyphenyl)methylidene]-3-oxobutanoate Chemical compound CCOC(=O)C(C(C)=O)=CC1=CC=CC=C1O GZFRHJPONRZEKP-UHFFFAOYSA-N 0.000 claims 1
- QHRKNRZYJVTILX-UHFFFAOYSA-N ethyl 2-acetyldec-2-enoate Chemical compound CCCCCCCC=C(C(C)=O)C(=O)OCC QHRKNRZYJVTILX-UHFFFAOYSA-N 0.000 claims 1
- QVLNMJLVSGGXOH-UHFFFAOYSA-N ethyl 2-acetylpent-2-enoate Chemical compound CCOC(=O)C(C(C)=O)=CCC QVLNMJLVSGGXOH-UHFFFAOYSA-N 0.000 claims 1
- KHCXKIQQZNPBDX-UHFFFAOYSA-N ethyl 2-hydroxy-3-(1h-imidazole-5-carbonyl)-4-oxopentanoate Chemical compound CCOC(=O)C(O)C(C(C)=O)C(=O)C1=CNC=N1 KHCXKIQQZNPBDX-UHFFFAOYSA-N 0.000 claims 1
- YQRAXLLUKHQLNQ-UHFFFAOYSA-N ethyl 3-acetyl-2-ethoxy-4-oxopentanoate Chemical compound CCOC(C(C(C)=O)C(C)=O)C(=O)OCC YQRAXLLUKHQLNQ-UHFFFAOYSA-N 0.000 claims 1
- 239000001257 hydrogen Substances 0.000 claims 1
- 229910052739 hydrogen Inorganic materials 0.000 claims 1
- 230000003472 neutralizing effect Effects 0.000 claims 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 1
- PMHBYAGKMHEFPA-UHFFFAOYSA-N triethyl ethene-1,1,2-tricarboxylate Chemical compound CCOC(=O)C=C(C(=O)OCC)C(=O)OCC PMHBYAGKMHEFPA-UHFFFAOYSA-N 0.000 claims 1
- MOMFXATYAINJML-UHFFFAOYSA-N 2-Acetylthiazole Chemical group CC(=O)C1=NC=CS1 MOMFXATYAINJML-UHFFFAOYSA-N 0.000 description 1
- FZGAAUKSGIREKE-UHFFFAOYSA-N CCCCCCC(=C(C(=O)C1=CC=C(C=C1)C(C)(C)C)C(=O)C2=CC=C(C=C2)OC)C Chemical compound CCCCCCC(=C(C(=O)C1=CC=C(C=C1)C(C)(C)C)C(=O)C2=CC=C(C=C2)OC)C FZGAAUKSGIREKE-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB0501237.2A GB0501237D0 (en) | 2005-01-21 | 2005-01-21 | Organic compounds |
| PCT/CH2006/000010 WO2006076821A1 (en) | 2005-01-21 | 2006-01-06 | 2 -c-substituted propane-1, 3 -dicarbonyl compounds and their use in neutralising malodour |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2008528451A JP2008528451A (ja) | 2008-07-31 |
| JP2008528451A5 true JP2008528451A5 (enExample) | 2009-02-19 |
Family
ID=34259438
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2007551527A Pending JP2008528451A (ja) | 2005-01-21 | 2006-01-06 | ２−ｃ置換プロパン−１，３−ジカルボニル化合物および悪臭中和におけるその使用 |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US20080305066A1 (enExample) |
| EP (1) | EP1838278A1 (enExample) |
| JP (1) | JP2008528451A (enExample) |
| KR (1) | KR20070097073A (enExample) |
| CN (1) | CN101106968A (enExample) |
| BR (1) | BRPI0614023A2 (enExample) |
| GB (1) | GB0501237D0 (enExample) |
| MX (1) | MX2007008551A (enExample) |
| WO (1) | WO2006076821A1 (enExample) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB0611770D0 (en) * | 2006-06-15 | 2006-07-26 | Givaudan Sa | Compounds |
| EP2272491A1 (fr) * | 2009-06-18 | 2011-01-12 | Robertet S.A. | Nouvelles compositions désodorisantes et produits désodorisants les renfermant |
| US8617528B2 (en) | 2010-12-06 | 2013-12-31 | Sytheon Ltd. | Compositions and methods for stabilizing ingredients using 2,4-pentanedione compounds |
| US8414870B2 (en) | 2010-12-06 | 2013-04-09 | Sytheon, Ltd. | Benzylidene substituted 2,4-pentanedione compounds and use thereof as stabilizers |
| US20120294821A1 (en) * | 2011-05-20 | 2012-11-22 | International Flavors & Fragrances Inc. | Low Volatile Reactive Malodor Counteractives and Methods of Use Thereof |
| US9126890B2 (en) * | 2011-10-20 | 2015-09-08 | International Flavors & Fragrances Inc. | Low volatile reactive malodor counteractives and methods of use thereof |
| US10226544B2 (en) | 2015-06-05 | 2019-03-12 | International Flavors & Fragrances Inc. | Malodor counteracting compositions |
| US10549003B2 (en) | 2016-05-31 | 2020-02-04 | The Procter & Gamble Company | Method of demonstrating efficacy of a malodor counteractant product |
| CN111432851B (zh) * | 2017-11-22 | 2023-06-23 | 弗门尼舍有限公司 | 挥发性成分限制或消除对恶臭的感知的用途 |
| BR112021018601A2 (pt) | 2019-03-20 | 2021-11-23 | Firmenich & Cie | Compostos pró-perfume encapsulados |
| CN114096651A (zh) | 2019-06-27 | 2022-02-25 | 弗门尼舍有限公司 | 已加香消费产品 |
| EP4039244A1 (en) | 2021-02-04 | 2022-08-10 | Givaudan SA | Improvements in or relating to organic compounds |
| US20250352446A1 (en) * | 2022-06-21 | 2025-11-20 | Firmenich Sa | Compositions for preventing, reducing, or ameliorating malodorous aldehydes and ketones, and uses thereof |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA970365A (en) * | 1972-07-14 | 1975-07-01 | Princeton Biomedix | Pharmaceutically useful compounds and methods of producing and using same |
| US4810819A (en) * | 1984-04-06 | 1989-03-07 | Zambon Spa | Process for the preparation of optically active alpha-acrylalkanoic acids and novel intermediates thereof |
| ATE35810T1 (de) * | 1984-04-06 | 1988-08-15 | Zambon Spa | Verfahren zur herstellung von optisch aktiven alpha-arylalkansaeuren und ihre zwischenprodukte. |
| DE3423249A1 (de) * | 1984-06-23 | 1986-01-02 | Hüls AG, 4370 Marl | Verfahren zur herstellung von alkyliden- und arylidenverbindungen |
| US4830787A (en) * | 1987-08-13 | 1989-05-16 | Nabisco Brands, Inc. | Low calorie fat mimetics comprising carboxy/carboxylate esters |
| JPH04202122A (ja) * | 1990-11-28 | 1992-07-22 | Procter & Gamble Co:The | ジケトン脱臭組成物及び脱臭方法 |
| SG91244A1 (en) * | 1996-06-24 | 2002-09-17 | Givaudan Roure Int | Malodour preventing agents |
| JP2000516517A (ja) * | 1996-08-19 | 2000-12-12 | ザ、プロクター、エンド、ギャンブル、カンパニー | β―ケトエステルプロフレグランスを含んだ臭気抑制組成物 |
| GB0320441D0 (en) * | 2003-09-02 | 2003-10-01 | Givaudan Sa | Organic compounds |
-
2005
- 2005-01-21 GB GBGB0501237.2A patent/GB0501237D0/en not_active Ceased
-
2006
- 2006-01-06 EP EP06700027A patent/EP1838278A1/en not_active Withdrawn
- 2006-01-06 WO PCT/CH2006/000010 patent/WO2006076821A1/en not_active Ceased
- 2006-01-06 MX MX2007008551A patent/MX2007008551A/es not_active Application Discontinuation
- 2006-01-06 JP JP2007551527A patent/JP2008528451A/ja active Pending
- 2006-01-06 US US11/814,057 patent/US20080305066A1/en not_active Abandoned
- 2006-01-06 BR BRPI0614023-8A patent/BRPI0614023A2/pt not_active IP Right Cessation
- 2006-01-06 CN CNA2006800028602A patent/CN101106968A/zh active Pending
- 2006-01-06 KR KR1020077016600A patent/KR20070097073A/ko not_active Ceased
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